ClinicalTrials.Veeva

Menu

Safety and Efficacy of Marqibo in Metastatic Malignant Uveal Melanoma

Spectrum Pharmaceuticals logo

Spectrum Pharmaceuticals

Status and phase

Completed
Phase 2

Conditions

Metastatic Malignant Uveal Melanoma

Treatments

Drug: Marqibo® (vincristine sulfate liposomes injection)

Study type

Interventional

Funder types

Industry

Identifiers

NCT00506142
HBS408 (formerly IST401)

Details and patient eligibility

About

Marqibo (liposomal vincristine) is a form of vincristine preparation. Vincristine is designed to interfere with the multiplication of cancer cells, which may slow or stop their growing and spreading throughout the body. This may cause the cancer cells to die. Liposomal vincristine is formed when vincristine is placed inside of oil droplets called liposomes, which may help to improve the delivery of drug to the tumor site. The liposomal formulation results in a slow, steady release of vincristine in the tumor metastasis, exposing the cancer cells to vincristine continuously.

The goal of this clinical research study is to learn if Marqibo (liposomal vincristine) can help to control metastatic uveal melanoma. The safety of liposomal vincristine will also be studied.

Approximately 50 patients will take part in this study.

Enrollment

54 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Uveal melanoma with histologic or cytologic confirmation of metastatic disease.
  • One unidimensionally measurable lesion. If this is a cutaneous lesion it must be at least 10 mm by caliper measure. If it is a visceral or nodal or soft tissue lesion, it must be >20 mm with conventional techniques or >10 mm with spiral CT scan. Bone lesions are not considered measurable.
  • Must not have received any prior systemic chemotherapy, immunotherapy, vaccine or hepatic arterial chemotherapy for metastatic disease.
  • Adequate liver, renal, and bone marrow function.
  • Zubrod performance status of 0-2.
  • Sign an informed consent form.

Exclusion criteria

  • Major surgery within 4 weeks of enrollment.
  • Advanced symptomatic central nervous system (CNS) involvement by melanoma and those on phenytoin or requiring steroids for brain metastases, spinal cord compression, or meningeal "carcinomatosis".
  • History of neurological disorders unrelated to chemotherapy (including familial neurological diseases and acquired demyelinating disorders).
  • Grade 2 or greater sensory, motor and/or autonomic neuropathy at screening from any cause.
  • Receiving treatment with drugs known to inhibit or induce hepatic drug metabolism by cytochrome P450-3A4 isoenzymes and/or P-glycoprotein within 1 week of study enrollment.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

54 participants in 2 patient groups

Cohort 1
Experimental group
Description:
Cohort 1 subjects will receive MARQIBO at a dose of 2.25 mg/m2 IV over 1 hour every 2 weeks.
Treatment:
Drug: Marqibo® (vincristine sulfate liposomes injection)
Cohort 2
Experimental group
Description:
Cohort 2 subjects will receive MARQIBO at a dose of 2.25 mg/m2 IV over 1 hour every week.
Treatment:
Drug: Marqibo® (vincristine sulfate liposomes injection)

Trial contacts and locations

4

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems